Job ID = 6368952 SRX = SRX7627553 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-16T00:35:50 prefetch.2.10.7: 1) Downloading 'SRR10961901'... 2020-06-16T00:35:50 prefetch.2.10.7: Downloading via HTTPS... 2020-06-16T00:36:27 prefetch.2.10.7: HTTPS download succeed 2020-06-16T00:36:27 prefetch.2.10.7: 'SRR10961901' is valid 2020-06-16T00:36:27 prefetch.2.10.7: 1) 'SRR10961901' was downloaded successfully Read 3682205 spots for SRR10961901/SRR10961901.sra Written 3682205 spots for SRR10961901/SRR10961901.sra fastq に変換しました。 bowtie でマッピング中... Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:00:53 3682205 reads; of these: 3682205 (100.00%) were unpaired; of these: 378258 (10.27%) aligned 0 times 2691200 (73.09%) aligned exactly 1 time 612747 (16.64%) aligned >1 times 89.73% overall alignment rate Time searching: 00:00:53 Overall time: 00:00:53 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 7 sequences. [bam_rmdupse_core] 2213007 / 3303947 = 0.6698 in library ' ' BAM に変換しました。 Bed ファイルを作成中... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Tue, 16 Jun 2020 09:38:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.bam'] # control file = None # effective genome size = 9.00e+07 # band width = 300 # model fold = [5, 50] # qvalue cutoff = 1.00e-05 # Larger dataset will be scaled towards smaller dataset. # Range for calculating regional lambda is: 10000 bps # Broad region calling is off # Paired-End mode is off INFO @ Tue, 16 Jun 2020 09:38:42: #1 read tag files... INFO @ Tue, 16 Jun 2020 09:38:42: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 09:38:49: 1000000 INFO @ Tue, 16 Jun 2020 09:38:49: #1 tag size is determined as 50 bps INFO @ Tue, 16 Jun 2020 09:38:49: #1 tag size = 50 INFO @ Tue, 16 Jun 2020 09:38:49: #1 total tags in treatment: 1090940 INFO @ Tue, 16 Jun 2020 09:38:49: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 09:38:49: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 16 Jun 2020 09:38:49: #1 tags after filtering in treatment: 1090940 INFO @ Tue, 16 Jun 2020 09:38:49: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 09:38:49: #1 finished! INFO @ Tue, 16 Jun 2020 09:38:49: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 09:38:49: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 09:38:49: #2 number of paired peaks: 851 WARNING @ Tue, 16 Jun 2020 09:38:49: Fewer paired peaks (851) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 851 pairs to build model! INFO @ Tue, 16 Jun 2020 09:38:49: start model_add_line... INFO @ Tue, 16 Jun 2020 09:38:49: start X-correlation... INFO @ Tue, 16 Jun 2020 09:38:49: end of X-cor INFO @ Tue, 16 Jun 2020 09:38:49: #2 finished! INFO @ Tue, 16 Jun 2020 09:38:49: #2 predicted fragment length is 53 bps INFO @ Tue, 16 Jun 2020 09:38:49: #2 alternative fragment length(s) may be 53,540 bps INFO @ Tue, 16 Jun 2020 09:38:49: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.05_model.r WARNING @ Tue, 16 Jun 2020 09:38:49: #2 Since the d (53) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 09:38:49: #2 You may need to consider one of the other alternative d(s): 53,540 WARNING @ Tue, 16 Jun 2020 09:38:49: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 09:38:49: #3 Call peaks... INFO @ Tue, 16 Jun 2020 09:38:49: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 09:38:52: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 09:38:53: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.05_peaks.xls INFO @ Tue, 16 Jun 2020 09:38:53: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 09:38:53: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.05_summits.bed INFO @ Tue, 16 Jun 2020 09:38:53: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (469 records, 4 fields): 2 millis CompletedMACS2peakCalling WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Tue, 16 Jun 2020 09:39:12: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.bam'] # control file = None # effective genome size = 9.00e+07 # band width = 300 # model fold = [5, 50] # qvalue cutoff = 1.00e-10 # Larger dataset will be scaled towards smaller dataset. # Range for calculating regional lambda is: 10000 bps # Broad region calling is off # Paired-End mode is off INFO @ Tue, 16 Jun 2020 09:39:12: #1 read tag files... INFO @ Tue, 16 Jun 2020 09:39:12: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 09:39:19: 1000000 INFO @ Tue, 16 Jun 2020 09:39:20: #1 tag size is determined as 50 bps INFO @ Tue, 16 Jun 2020 09:39:20: #1 tag size = 50 INFO @ Tue, 16 Jun 2020 09:39:20: #1 total tags in treatment: 1090940 INFO @ Tue, 16 Jun 2020 09:39:20: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 09:39:20: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 16 Jun 2020 09:39:20: #1 tags after filtering in treatment: 1090940 INFO @ Tue, 16 Jun 2020 09:39:20: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 09:39:20: #1 finished! INFO @ Tue, 16 Jun 2020 09:39:20: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 09:39:20: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 09:39:20: #2 number of paired peaks: 851 WARNING @ Tue, 16 Jun 2020 09:39:20: Fewer paired peaks (851) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 851 pairs to build model! INFO @ Tue, 16 Jun 2020 09:39:20: start model_add_line... INFO @ Tue, 16 Jun 2020 09:39:20: start X-correlation... INFO @ Tue, 16 Jun 2020 09:39:20: end of X-cor INFO @ Tue, 16 Jun 2020 09:39:20: #2 finished! INFO @ Tue, 16 Jun 2020 09:39:20: #2 predicted fragment length is 53 bps INFO @ Tue, 16 Jun 2020 09:39:20: #2 alternative fragment length(s) may be 53,540 bps INFO @ Tue, 16 Jun 2020 09:39:20: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.10_model.r WARNING @ Tue, 16 Jun 2020 09:39:20: #2 Since the d (53) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 09:39:20: #2 You may need to consider one of the other alternative d(s): 53,540 WARNING @ Tue, 16 Jun 2020 09:39:20: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 09:39:20: #3 Call peaks... INFO @ Tue, 16 Jun 2020 09:39:20: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 09:39:22: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 09:39:24: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.10_peaks.xls INFO @ Tue, 16 Jun 2020 09:39:24: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 09:39:24: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.10_summits.bed INFO @ Tue, 16 Jun 2020 09:39:24: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (239 records, 4 fields): 1 millis CompletedMACS2peakCalling BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Tue, 16 Jun 2020 09:39:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.bam'] # control file = None # effective genome size = 9.00e+07 # band width = 300 # model fold = [5, 50] # qvalue cutoff = 1.00e-20 # Larger dataset will be scaled towards smaller dataset. # Range for calculating regional lambda is: 10000 bps # Broad region calling is off # Paired-End mode is off INFO @ Tue, 16 Jun 2020 09:39:42: #1 read tag files... INFO @ Tue, 16 Jun 2020 09:39:42: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 09:39:49: 1000000 INFO @ Tue, 16 Jun 2020 09:39:49: #1 tag size is determined as 50 bps INFO @ Tue, 16 Jun 2020 09:39:49: #1 tag size = 50 INFO @ Tue, 16 Jun 2020 09:39:49: #1 total tags in treatment: 1090940 INFO @ Tue, 16 Jun 2020 09:39:49: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 09:39:49: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 16 Jun 2020 09:39:49: #1 tags after filtering in treatment: 1090940 INFO @ Tue, 16 Jun 2020 09:39:49: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 09:39:49: #1 finished! INFO @ Tue, 16 Jun 2020 09:39:49: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 09:39:49: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 09:39:49: #2 number of paired peaks: 851 WARNING @ Tue, 16 Jun 2020 09:39:49: Fewer paired peaks (851) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 851 pairs to build model! INFO @ Tue, 16 Jun 2020 09:39:49: start model_add_line... INFO @ Tue, 16 Jun 2020 09:39:49: start X-correlation... INFO @ Tue, 16 Jun 2020 09:39:49: end of X-cor INFO @ Tue, 16 Jun 2020 09:39:49: #2 finished! INFO @ Tue, 16 Jun 2020 09:39:49: #2 predicted fragment length is 53 bps INFO @ Tue, 16 Jun 2020 09:39:49: #2 alternative fragment length(s) may be 53,540 bps INFO @ Tue, 16 Jun 2020 09:39:49: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.20_model.r WARNING @ Tue, 16 Jun 2020 09:39:49: #2 Since the d (53) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 09:39:49: #2 You may need to consider one of the other alternative d(s): 53,540 WARNING @ Tue, 16 Jun 2020 09:39:49: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 09:39:49: #3 Call peaks... INFO @ Tue, 16 Jun 2020 09:39:49: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 09:39:52: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 09:39:53: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.20_peaks.xls INFO @ Tue, 16 Jun 2020 09:39:53: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 09:39:53: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7627553/SRX7627553.20_summits.bed INFO @ Tue, 16 Jun 2020 09:39:53: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (89 records, 4 fields): 1 millis CompletedMACS2peakCalling